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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >D2 receptor-mediated inhibition of GABA release by endogenous dopamine in the rat globus pallidus.
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D2 receptor-mediated inhibition of GABA release by endogenous dopamine in the rat globus pallidus.

机译:D2受体介导的大鼠苍白球内源性多巴胺抑制GABA释放。

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摘要

Attempting to better understand the role of the dopaminergic innervation in the rat globus pallidus, we examined here whether or not endogenous dopamine modulates the release of [3H]GABA in superfused pallidal slices. The superfusion medium contained elevated (15 mM) potassium. The release of endogenous dopamine was induced by the dopamine releaser drug, methamphetamine. Methamphetamine (100 microM) inhibited by 46% the release of [3H]GABA. Methamphetamine inhibition was completely blocked by reserpinization of the rats. It was also completely blocked by the D2 dopamine receptor antagonist sulpiride (10 microM). Sulpiride alone caused a 105% increase in GABA release. The increase was not observed in slices from reserpinized rats. Quinpirole (10 microM), a D2 dopamine receptor agonist, inhibited (43%) [3H]GABA release. The results suggest that endogenous dopamine exerts an inhibitory effect on GABA release in the rat globus pallidus. The effect is mediated by D2 receptors presumably located on striatopallidal axon terminals.
机译:为了更好地理解多巴胺能神经支配在大鼠苍白球中的作用,我们在这里检查了内源性多巴胺是否调节了融合的苍白片中[3H] GABA的释放。超融合培养基含有升高的(15 mM)钾。多巴胺释放药物甲基苯丙胺可诱导内源性多巴胺的释放。甲基苯丙胺(100 microM)抑制[3H] GABA的释放46%。甲基苯丙胺的抑制作用被大鼠的再固定化完全阻断。它也被D2多巴胺受体拮抗剂舒必利(10 microM)完全阻断。单独使用舒必利会导致GABA释放增加105%。在再固定化大鼠的切片中未观察到增加。 D2多巴胺受体激动剂喹吡罗(10 microM)抑制(43%)[3H] GABA释放。结果表明内源性多巴胺对大鼠苍白球GABA释放具有抑制作用。该作用由大概位于纹状体外胚层轴突末端的D2受体介导。

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